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1.
ACS Nano ; 2024 Jun 03.
Article in English | MEDLINE | ID: mdl-38829730

ABSTRACT

Phase heterogeneity of bromine-iodine (Br-I) mixed wide-bandgap (WBG) perovskites has detrimental effects on solar cell performance and stability. Here, we report a heterointerface anchoring strategy to homogenize the Br-I distribution and mitigate the segregation of Br-rich WBG-perovskite phases. We find that methoxy-substituted phenyl ethylammonium (x-MeOPEA+) ligands not only contribute to the crystal growth with vertical orientation but also promote halide homogenization and defect passivation near the buried perovskite/hole transport layer (HTL) interface as well as reduce trap-mediated recombination. Based on improvements in WBG-perovskite homogeneity and heterointerface contacts, NiOx-based opaque WBG-perovskite solar cells (WBG-PSCs) achieved impressive open-circuit voltage (Voc) and fill factor (FF) values of 1.22 V and 83%, respectively. Moreover, semitransparent WBG-PSCs exhibit a PCE of 18.5% (15.4% for the IZO front side) and a high FF of 80.7% (79.4% for the IZO front side) for a designated illumination area (da) of 0.12 cm2. Such a strategy further enables 24.3%-efficient two-terminal perovskite/silicon (double-polished) tandem solar cells (da of 1.159 cm2) with a high Voc of over 1.90 V. The tandem devices also show high operational stability over 1000 h during T90 lifetime measurements.

2.
ACS Appl Mater Interfaces ; 16(15): 19838-19848, 2024 Apr 17.
Article in English | MEDLINE | ID: mdl-38569046

ABSTRACT

Environment-friendly antisolvents are critical for obtaining highly efficient, reproducible, and sustainable perovskite solar cells (PSCs). Here, we introduced a green mixture antisolvent of ethyl acetate-isopropanol (EA/IPA) to finely regulate the crystal grain growth and related film properties, including the morphology, crystal structure, and chemical composition of the perovskite thin film. The IPA with suitable content in EA plays a key role in achieving a smooth and compact high-quality perovskite thin film, leading to the suppression of film defect-induced nonradiative recombination. As a result, the PSCs based on the EA/IPA (5:1) antisolvent showed a power conversion efficiency of 22.9% with an open-circuit voltage of 1.17 V.

3.
Ann Clin Lab Sci ; 53(2): 271-277, 2023 Mar.
Article in English | MEDLINE | ID: mdl-37094865

ABSTRACT

OBJECTIVE: DEAD-box helicase 49 (DDX49) functions as an RNA helicase and is involved in oncogenic transformation of cells. In this study, the pathological role of DDX49 in cervical cancer (CC) was investigated. METHODS: Cell proliferation was detected using EdU staining and MTT assays. Cell invasion and migration were detected by transwell, and flow cytometry was performed to assess cell cycle and apoptosis. RESULTS: DDX49 was elevated in CC tissues based on UCLCAN analysis. Knockdown of DDX49 reduced cell viability, proliferation, invasion and migration of CC cells, while over-expression of DDX49 promoted the proliferation and metastasis of CC cells. Silencing of DDX49 stimulated cell apoptosis of CC cells, and induced cell cycle arrest at G0/G1 phase. However, over-expression of DDX49 stimulated cell cycle progression of CC, and suppressed the cell apoptosis. Loss of DDX49 decreased protein expression of ß-catenin, GSK3ß, p-AKT and p-PI3K in CC cells, while ectopically expression of DDX49 enhanced the expression of ß-catenin, GSK3ß, p-AKT and p-PI3K. CONCLUSION: DDX49 deficiency exerted anti-tumor effect on CC through inactivation of PI3K/AKT and Wnt/ß-catenin pathways.


Subject(s)
Proto-Oncogene Proteins c-akt , Uterine Cervical Neoplasms , Female , Humans , Proto-Oncogene Proteins c-akt/metabolism , Glycogen Synthase Kinase 3 beta/metabolism , Cell Line, Tumor , Phosphatidylinositol 3-Kinases/metabolism , Uterine Cervical Neoplasms/metabolism , beta Catenin/genetics , Cell Proliferation/genetics , Cell Movement/genetics , Gene Expression Regulation, Neoplastic , Apoptosis/genetics
4.
Nanomicro Lett ; 15(1): 117, 2023 Apr 30.
Article in English | MEDLINE | ID: mdl-37121982

ABSTRACT

NiOx-based inverted perovskite solar cells (PSCs) have presented great potential toward low-cost, highly efficient and stable next-generation photovoltaics. However, the presence of energy-level mismatch and contact-interface defects between hole-selective contacts (HSCs) and perovskite-active layer (PAL) still limits device efficiency improvement. Here, we report a graded configuration based on both interface-cascaded structures and p-type molecule-doped composites with two-/three-dimensional formamidinium-based triple-halide perovskites. We find that the interface defects-induced non-radiative recombination presented at HSCs/PAL interfaces is remarkably suppressed because of efficient hole extraction and transport. Moreover, a strong chemical interaction, halogen bonding and coordination bonding are found in the molecule-doped perovskite composites, which significantly suppress the formation of halide vacancy and parasitic metallic lead. As a result, NiOx-based inverted PSCs present a power-conversion-efficiency over 23% with a high fill factor of 0.84 and open-circuit voltage of 1.162 V, which are comparable to the best reported around 1.56-electron volt bandgap perovskites. Furthermore, devices with encapsulation present high operational stability over 1,200 h during T90 lifetime measurement (the time as a function of PCE decreases to 90% of its initial value) under 1-sun illumination in ambient-air conditions.

5.
Biomed Res Int ; 2022: 5823276, 2022.
Article in English | MEDLINE | ID: mdl-36277878

ABSTRACT

In order to investigate the effects of clopidogrel rehabilitation on the levels of cardiac protein kinase C (PKC), cardiac heat shock protein 70 (HSP70), and cardiac index (CI) in rats with myocardial ischemia-reperfusion injury (MIRI), sixty Wistar rats are randomly divided into three groups (sham operation group, model group, and clopidogrel group), with 20 rats in each group. The clopidogrel group is given clopidogrel by gavage, and the sham operation group and the model group are given the same amount of normal saline by gavage. The experimental results show that compared with the model group, the clopidogrel group has clear horizontal lines and cell edema. The myocardial infarction rate, creatine kinase-MB (CK-MB), and malondialdehyde (MDA) of the model group and clopidogrel group in the control sham operation group significantly increase.


Subject(s)
Myocardial Reperfusion Injury , Animals , Rats , Clopidogrel , Creatine Kinase , HSP70 Heat-Shock Proteins/metabolism , Malondialdehyde , Myocardial Reperfusion Injury/drug therapy , Protein Kinase C , Rats, Wistar
6.
Comput Math Methods Med ; 2022: 2172412, 2022.
Article in English | MEDLINE | ID: mdl-35479188

ABSTRACT

Ulinastatin, a common adjuvant drug in the clinical treatment of acute circulatory failure, has a good effect on various inflammatory diseases. In this study, we aim to explore the clinical efficacy of ulinastatin combined with meglumine adenosine cyclophosphate in patients with acute myocardial infarction (AMI) and its effect on cardiac function and endothelial function of patients. 100 AMI patients treated in our hospital (February 2020-October 2020) were randomly chosen and divided into group J and group Q, with 50 cases in each group. Group Q was treated with meglumine adenosine cyclophosphate only, while group J was treated with ulinastatin combined with meglumine adenosine cyclophosphate to compare the treatment efficiency, cardiac structure indexes, cardiac systolic function, blood lipid levels, vascular endothelial function, QLI (quality of life) scores, BI indexes, and FMA (motor function) scores between the two groups. The treatment efficiency, QLI score, BI index, and FMA score in group J were notably higher compared with group Q (P < 0.05). The cardiac structure indexes, cardiac systolic function, blood lipid level, and vascular endothelial function in group J were notably better compared with group Q (P < 0.05). Ulinastatin combined with meglumine adenosine cyclophosphate can obviously enhance the therapeutic effect of AMI patients and improve the endothelial function and cardiac function of patients, which is very promising in this medical area.


Subject(s)
Adenosine , Myocardial Infarction , Adenosine/therapeutic use , Glycoproteins , Humans , Meglumine/therapeutic use , Myocardial Infarction/drug therapy , Quality of Life , Treatment Outcome
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